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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Pyridinecarboxamide, 5-bromo-N-methoxy-N-methyl-

CON(C(=O)c1cncc(c1)Br)C Request for Quotation
Chemical Name: 3-Pyridinecarboxamide, 5-bromo-N-methoxy-N-methyl-
CAS Number: 183608-47-1
Product Number: AG0027R0(AGN-PC-01WIJK)
Synonyms:
MDL No:
Molecular Formula: C8H9BrN2O2
Molecular Weight: 245.0733

Identification/Properties

Computed Properties
Molecular Weight:
245.076g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
243.985g/mol
Monoisotopic Mass:
243.985g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
189
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P301+P312+P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-N-methoxy-N-methylnicotinamide, also known as $name$, serves as a versatile chemical reagent in organic synthesis due to its unique properties. This compound acts as a valuable building block in the synthesis of various biologically active molecules and pharmaceutical intermediates. Its capacity to undergo selective transformations makes it an essential component in the development of new drug candidates and functional materials. In chemical synthesis, $name$ is frequently utilized as a protecting group for amines, enabling precise control over reactions and facilitating the formation of complex molecular structures. Furthermore, its inherent stability and compatibility with a wide range of reaction conditions render it a valuable tool for synthetic chemists seeking to streamline processes and enhance overall efficiency. Through strategic incorporation into synthetic pathways, 5-Bromo-N-methoxy-N-methylnicotinamide enables the synthesis of diverse compounds with enhanced properties and targeted functionalities, making it a fundamental ingredient in modern chemical synthesis strategies.